Sura O. Hussein

Doha, DA, Qatar

Last Updated: 09/26/2026

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Found 11 publications

RETICULOCYTE SUBPOPULATION ANALYSIS AND ITS CORRELATION WITH IRON DEFICIENCY ANEMIA: A RETROSPECTIVE STUDY IN A PREDOMINANTLY FEMALE POPULATION.

RETICULOCYTE SUBPOPULATION ANALYSIS AND ITS CORRELATION WITH IRON DEFICIENCY ANEMIA: A RETROSPECTIVE STUDY IN A PREDOMINANTLY FEMALE POPULATION.

Journal: Georgian medical news
Published: May 02, 2026

BIOCHEMICAL ASSOCIATION BETWEEN CALCIUM HOMEOSTASIS AND SERUM URIC ACID LEVELS IN PATIENTS WITH HYPOTHYROIDISM: A COMPARATIVE EVALUATION WITH 25-HYDROXYVITAMIN D.

BIOCHEMICAL ASSOCIATION BETWEEN CALCIUM HOMEOSTASIS AND SERUM URIC ACID LEVELS IN PATIENTS WITH HYPOTHYROIDISM: A COMPARATIVE EVALUATION WITH 25-HYDROXYVITAMIN D.

Journal: Georgian medical news
Published: February 13, 2026

SERUM TSH, FT3, FT4, AND FASTING BLOOD GLUCOSE LEVELS TO INVESTIGATE THE ASSOCIATION BETWEEN THYROID DYSFUNCTION AND TYPE 2 DIABETES MELLITUS.

SERUM TSH, FT3, FT4, AND FASTING BLOOD GLUCOSE LEVELS TO INVESTIGATE THE ASSOCIATION BETWEEN THYROID DYSFUNCTION AND TYPE 2 DIABETES MELLITUS.

Journal: Georgian medical news
Published: July 30, 2025

ASSOCIATION BETWEEN MICROALBUMINURIA AND THYROID DYSFUNCTION COMPARED TO DIABETIC KIDNEY DISEASE PROGRESSION IN TYPE 2 DIABETES MELLITUS PATIENTS.

ASSOCIATION BETWEEN MICROALBUMINURIA AND THYROID DYSFUNCTION COMPARED TO DIABETIC KIDNEY DISEASE PROGRESSION IN TYPE 2 DIABETES MELLITUS PATIENTS.

Journal: Georgian medical news
Published: July 30, 2025

Biallelic Loss-of-Function Variant in MINPP1 Causes Pontocerebellar Hypoplasia with Characteristic Severe Neurodevelopmental Disorder.

Biallelic Loss-of-Function Variant in MINPP1 Causes Pontocerebellar Hypoplasia with Characteristic Severe Neurodevelopmental Disorder.

Journal: International journal of molecular sciences
Published: March 28, 2025

ASSOCIATION BETWEEN GLYCATED HEMOGLOBIN AND ELEVATED THYROID HORMONES LEVELS IN PATIENTS WITH TYPE 2 DIABETES MELLITUS.

ASSOCIATION BETWEEN GLYCATED HEMOGLOBIN AND ELEVATED THYROID HORMONES LEVELS IN PATIENTS WITH TYPE 2 DIABETES MELLITUS.

Journal: Georgian medical news
Published: February 26, 2025

Integrating Genome Sequencing and Untargeted Metabolomics in Monozygotic Twins with a Rare Complex Neurological Disorder.

Integrating Genome Sequencing and Untargeted Metabolomics in Monozygotic Twins with a Rare Complex Neurological Disorder.

Journal: Metabolites
Published: February 04, 2024

A loss-of-function AGTR1 variant in a critically-ill infant with renal tubular dysgenesis: case presentation and literature review.

A loss-of-function AGTR1 variant in a critically-ill infant with renal tubular dysgenesis: case presentation and literature review.

Journal: BMC nephrology
Published: November 28, 2023

Association between oxidative stress, antioxidant enzymes, and homocysteine in patients with polycystic ovary syndrome.

Association between oxidative stress, antioxidant enzymes, and homocysteine in patients with polycystic ovary syndrome.

Journal: European review for medical and pharmacological sciences
Published: November 17, 2023

Genomic architecture of autism spectrum disorder in Qatar: The BARAKA-Qatar Study.

Genomic architecture of autism spectrum disorder in Qatar: The BARAKA-Qatar Study.

Journal: Genome medicine
Published: March 02, 2023

Patterns and distribution of de novo mutations in multiplex Middle Eastern families.

Patterns and distribution of de novo mutations in multiplex Middle Eastern families.

Journal: Journal of human genetics
Published: February 01, 2022
Showing 1-11 of 11

Last Updated: 09/26/2026